Conversion of cyclopentadienyl silyl amines to organometallic complexes comprising titanium bisalkoxy moiety or titanium dichloride moiety

ABSTRACT

Conversion of cyclopentadienyl or indenyl compounds to titanium organometallic complexes by treatment with titanium tetraalkoxides is described.

FIELD OF THE INVENTION

[0001] This invention relates to titanium organometallic complexes whichcomprise a titanium bisalkoxy moiety or a titanium dichloride moiety.

BACKGROUND OF THE INVENTION

[0002] U.S. Pat. Nos. 5,491,246 and 5,504,223 describe the treatment ofMe₄C₅SiMe₂N^(t)-bu[MgCl]₂(DME)_(n) with titanium tetraisopropoxide toprovide Me₄C₅SiMe₂N^(t)-buTi(OiPr)₂ which may be treated with SiCl₄ toyield the corresponding dichloride.

DEFINITIONS

[0003] In this specification, the following expressions have themeanings set forth hereinafter:

[0004] (1) Cyclopentadienyl means any substituted or unsubstitutedcyclopentadienyl compound, group or moiety, including but not limited toany alkylcyclopentadienyl, any indenyl, or any alkyl indenyl compound,group or moiety having one or more C₁ to C₁₀ alkyl ring substituents.

[0005] (2) Alkoxide means any radical or group having the formula —OR,wherein R is an alkyl group.

[0006] (3) Cyclopentadienyl silyl amine means a compound of Formula

[0007] in which Z is a cyclopentadienyl group or moiety and each of R¹,R² and R³ is independently, the same or a different alkyl group,preferably a C₁ to C₁₀ alkyl group.

SUMMARY OF THE INVENTION

[0008] Pursuant to this invention, an alkali metallide of acyclopentadienyl silyl amine is reacted with a titanium tetraalkoxide(Ti(OR)₄) in which R is a C₁ to C₁₀ alkyl group, preferably an isopropylgroup. The reaction mixture contains the desired bisalkoxide and, as aby-product, an alkali metal alkoxide which may be isolated or convertedin situ to an insoluble alkali metal halide to facilitate removal byfiltration. The filtrate contains the desired bisalkoxide which may beconverted to the corresponding dichloride by treatment with ahalogenating agent, e.g., SiCl₄.

DESCRIPTION OF THE INVENTION

[0009] The treatment of a silyl amine with Ti(OR)₄ may be accomplishedin any solvent or medium in which the desired titanium bisalkoxide issoluble. Preferred solvents or media are about 10% to 25% by weightmixtures of ethyl ether and a C₆ to C₈ hydrocarbon. The treatment may beaccomplished at a temperature of from about −20° to −10° C. Theconversion of the alkali metal alkoxide by-product to an alkali metalhalide insoluble in the solvent contained in the titanium bisalkoxidesynthesis reaction mixture is appropriately conducted at a temperatureof from about −35° to −20° C. Conversion of the bisalkoxide to thecorresponding dichloride may be accomplished in situ in the synthesisreaction mixture at a temperature of −20° C. to room temperature orreflexing temperature. Useful halogenating agents include SiCl₄, BCl₃,and AlCl₃.

EXAMPLE 1

[0010]2-Me-indenyl SiMe₂NH^(t)Bu is dilithiated by treatment withbutyllithium, e.g., in a 50 weight percent hexane/ether medium at −20°C. See Equation 1:

[0011] The dilithiated silyl amine is treated with titaniumtetraisopropoxide at a temperature of −35° C., wherein a reactionmixture comprising indenyl SiMe₂NH^(t)Bu titanium isopropoxide andlithium isopropoxide is produced. See Equation 2:

[0012] The reaction mixture is treated with SiCl₄ in an amount, e.g.,0.6 equiv, sufficient to convert LiOiPR in situ to LiCl which is removedby filtration. A hexane wash of the cake may be combined with the motherliquor which is a solution of the desired titanium bisisopropoxidecomplex in hexanes/ether.

[0013] 1.5 equivalents of SiCl₄ are added to the LiCl-free mother liquorwhich contains the titanium bis(isopropoxide) complex to provide asecond reaction mixture which is refluxed for six hours, and cooled toprecipitate the desired titanium dichloride complex for removal byfiltration. The cake is washed with hexanes. Titanium dichloride complexyield=70% to 80% (based on the silyl amine).

We claim:
 1. A method which comprises: (i) providing a first reactionmixture comprising a solution of a titanium bisalkoxide complex and analkali metal alkoxide, wherein said step (i) first reaction mixture isprovided by treating a cyclopentadienyl silyl amine metallide with atitanium tetraalkoxide in a non-interfering medium in which saidtitanium bisalkoxide complex and said alkali metal alkoxide are soluble,(ii) treating said alkali metal alkoxide in said first reaction mixturewith a halogenating agent to produce a second reaction mixture whereinsaid alkali metal alkoxide is converted to an alkali metal halideinsoluble in said step (i) non-interfering medium contained in saidfirst reaction mixture, and (iii) removing said insoluble alkali metalhalide from said second reaction mixture wherein a mother liquorcontaining a solution of said titanium bisalkoxide complex in said step(i) non-interfering medium is produced.
 2. The method of claim 1 furthercomprising a step (iv) treating said step (iii) solution of saidtitanium bisalkoxide complex with a halogenating agent wherein a secondreaction mixture comprising an organometallic complex including atitanium dihalide moiety is produced.
 3. The method of claim 1 whereinsaid step (i) cyclopentadienyl silyl amine alkali metallide is lithiated2-methyl indenyl SiMe₂NH^(t)bu.
 4. In a method wherein acyclopentadienyl compound is treated in a non-interfering medium with atitanium tetraalkoxide and wherein said treatment provides a reactionmixture comprising a cyclopentadienyl bisalkoxide and an alkali metalalkoxide in solution in said non-interfering medium, the improvementwhich comprises converting said alkali metal alkoxide in saidnon-interfering medium to an alkali metal halide.
 5. The claim 1 methodwherein said titanium tetraalkoxide has the formula Ti(OR)₄ in which Ris an alkyl group.
 6. The claim 1 method wherein step (i) treating isaccomplished at a temperature of −35° to −20° C.
 7. The claim 4 methodin which said cyclopentadienyl compound is an alkyl cyclopentadienylcompound having at least one C₁ to C₁₀ alkyl ring substituent.